Alkanes AS Flashcards

1
Q

What are alkanes?

A

Saturated hydrocarbons with the general formula CₙH₂ₙ₊₂.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is petroleum?

A

A mixture mainly consisting of alkane hydrocarbons.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How is crude oil separated?

A

Crude oil is vaporized and fed through a column that is hotter at the bottom and cooler at the top, allowing fractions to be collected based on boiling points.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is thermal cracking?

A

A process that takes place at high temperatures (up to 1000°C) and pressures (up to 70 atm) to produce alkenes from long-chain alkanes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is catalytic cracking?

A

A process that occurs at around 500°C and slight pressure in the presence of a zeolite catalyst, mainly producing motor fuels and aromatic hydrocarbons.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Why do alkanes have specific boiling points?

A

Their boiling points depend on chain length and branching; longer chains have more Van der Waals forces, leading to higher boiling points.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the equation for complete combustion of alkanes?

A

A: CₙH₂ₙ₊₂ + O₂ → CO₂ + H₂O.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the equation for incomplete combustion of alkanes?

A

CₙH₂ₙ₊₂ + O₂ → CO + H₂O.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the issues with CO₂?

A

It is a greenhouse gas that contributes to global warming; solutions include burning less fossil fuel.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the problems associated with CO?

A

Carbon monoxide is toxic; ensure a good supply of air/oxygen during combustion to minimize this.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the problems caused by soot?

A

Soot can blacken buildings and contribute to global dimming; solutions include ensuring adequate air supply during combustion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What problems does sulfur dioxide cause?

A

It leads to acid rain, damaging trees, buildings, and aquatic life; solutions include removing sulfur from fuels or desulfurizing flue gases.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How are nitrogen oxides formed?

A

Through the reaction of nitrogen and oxygen at high temperatures, often in engines; they also contribute to acid rain.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is flue gas desulfurization?

A

A process using alkaline slurry (e.g., calcium carbonate) to remove SO₂ from flue gases, forming harmless calcium sulfate.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is a free radical?

A

A highly reactive particle with an unpaired electron, formed when a covalent bond splits.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How is ozone formed in the stratosphere?

A

UV radiation splits oxygen molecules into free radicals, which react with other oxygen molecules to form O₃.

17
Q

What are CFCs and why are they banned?

A

CFCs are inert halogenoalkanes that deplete the ozone layer; they were banned due to their harmful environmental effects.

18
Q

What are some alternatives to CFCs?

A

Hydrofluorocarbons (HFCs) and hydrocarbons are safer substitutes now used in refrigeration and aerosol propellants.

19
Q

What is a halogenoalkane?

A

A halogenoalkane is an alkane with at least one halogen atom in place of a hydrogen atom.

20
Q

What are some common uses of halogenoalkanes?

A

Halogenoalkanes are used as solvents, pharmaceuticals, refrigerators, and propellants.

21
Q

What is the general formula for mono-substituted halogenoalkanes?

A

CnH2n+1X, where X is a halogen.

22
Q

Why is the carbon-halogen bond in a halogenoalkane polar?

A

Halogens are much more electronegative than carbon, making the carbon atom electron-deficient and prone to attack by nucleophiles.

23
Q

What are nucleophiles?

A

Nucleophiles are electron-pair donors that attack electron-deficient carbon atoms. Examples include OH-, CN-, and NH3.

24
Q

What occurs during the hydrolysis of halogenoalkanes?

A

When halogenoalkanes react with an aqueous solution of warm hydroxide ions (OH-) and water, they produce an alcohol and a halide ion.

25
Q

What is the role of hydroxide ions in the hydrolysis of halogenoalkanes?

A

Hydroxide ions (OH-) donate lone pairs to the electron-deficient carbon, leading to the formation of a covalent bond and the breaking of the carbon-halogen bond.

26
Q

What is formed when halogenoalkanes react with ethanolic potassium cyanide (KCN)?

A

A nitrile is formed.

27
Q

What is the result of reacting a halogenoalkane with excess ethanolic ammonia?

A

An amine is formed.

28
Q

What determines the rate of hydrolysis of halogenoalkanes?

A

The strength of the C-Halogen bond. The C-F bond is the strongest, so fluoroalkanes react slower, while the C-I bond is the weakest, so iodoalkanes react faster.

29
Q

What type of reaction occurs when halogenoalkanes react with hydroxide ions dissolved in ethanol?

A

An elimination reaction, forming an alkene.

30
Q

What are the main mechanisms for halogenoalkane reactions based on their structure?

A
  • Primary Haloalkanes: Mainly undergo nucleophilic substitution.
  • Secondary Haloalkanes: Can undergo both substitution and elimination.
  • Tertiary Haloalkanes: Mainly undergo elimination.